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Long Non-Coding TP73-AS1: A Potential Biomarker and Therapeutic Target in Cancer
Kejing Li1,2, Dapeng Zhao2,3,4, Xuena Liu2,3,4
1School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, China.
Abstract:
Tumor protein 73 antisense RNA 1 (TP73-AS1), a newly discovered long non-coding RNA (lncRNA), the dysregulated expression of which is closely related to the occurrence, drug resistance, and prognosis of various cancers. Exploring the regulatory mechanism of TP73-AS1 provides a new research direction for cancer diagnosis and treatment. On this basis, we briefly review the molecular structural and dual regulatory roles of TP73-AS1 in cancer. In addition, we outline its three molecular mechanisms in cancer: binding to proteins, regulating signaling pathways, and serving as molecular sponges. Subsequently, we introduce the role of TP73-AS1 in common malignant tumors such as gastric cancer (GC), lung cancer, colorectal cancer (CRC), etc. Last, emphasis is given to the potential clinical value of TP73-AS1, especially as single nucleotide polymorphisms of this lncRNA are associated with the risk of GC and CRC. Therefore, this review highlights the significance of TP73-AS1 as a novel biomarker and therapeutic target.
Insights
Tumor protein 73 antisense RNA 1 (TP73-AS1) is a long non-coding RNA implicated in cancer development and drug resistance. Its regulatory mechanisms and clinical potential as a biomarker and therapeutic target are reviewed.
Area of Science:
- * Molecular oncology
- * Cancer genomics
- * RNA biology
Background:
- * Tumor protein 73 antisense RNA 1 (TP73-AS1) is a long non-coding RNA (lncRNA) with dysregulated expression in various cancers.
- * Aberrant TP73-AS1 expression correlates with cancer occurrence, drug resistance, and patient prognosis.
- * Understanding TP73-AS1's regulatory roles offers new avenues for cancer diagnosis and treatment.
Purpose of the Study:
- * To review the molecular structure and dual regulatory functions of TP73-AS1 in cancer.
- * To elucidate the molecular mechanisms through which TP73-AS1 influences cancer progression.
- * To highlight the clinical significance and therapeutic potential of TP73-AS1 in oncology.
Main Methods:
- * Literature review of existing studies on TP73-AS1 in cancer.
- * Analysis of TP73-AS1's molecular interactions, including protein binding and signaling pathway regulation.
- * Examination of TP73-AS1's role as a molecular sponge for microRNAs.
- * Compilation of data on TP73-AS1's involvement in specific cancers like gastric, lung, and colorectal cancer.
Main Results:
- * TP73-AS1 exhibits diverse molecular mechanisms in cancer, including protein binding, signaling pathway modulation, and acting as a molecular sponge.
- * TP73-AS1 plays a significant role in the pathogenesis of common malignancies such as gastric cancer (GC), lung cancer, and colorectal cancer (CRC).
- * Single nucleotide polymorphisms (SNPs) in TP73-AS1 are associated with increased risk for GC and CRC.
Conclusions:
- * TP73-AS1 is a crucial player in cancer development and progression through multiple molecular pathways.
- * TP73-AS1 demonstrates significant potential as a diagnostic biomarker and a therapeutic target for various cancers.
- * Further research into TP73-AS1's functions could lead to novel clinical strategies for cancer management.
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